Canonical Allele Identifier: CA1977488057

Gene: FADS3

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61887425_61887426delinsCT , CM000673.2:g.61887425_61887426delinsCT	GRCh38
NC_000011.9:g.61654897_61654898delinsCT , CM000673.1:g.61654897_61654898delinsCT	GRCh37
NC_000011.8:g.61411473_61411474delinsCT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278829.7:c.213+3743_213+3744delinsAG MANE Select	ENSP00000278829.2:n.213+3743_213+3744delinsAG
ENST00000278829.6:c.213+3743_213+3744delinsAG	ENSP00000278829.2:n.213+3743_213+3744delinsAG
ENST00000414624.6:n.286+3743_286+3744delinsAG
ENST00000525588.5:c.213+3743_213+3744delinsAG	ENSP00000432206.1:n.213+3743_213+3744delinsAG
ENST00000527697.5:c.-160+4433_-160+4434delinsAG	ENSP00000431533.1:n.-160+4433_-160+4434delinsAG
NM_021727.4:c.213+3743_213+3744delinsAG	NP_068373.1:n.213+3743_213+3744delinsAG
XM_011545023.1:c.213+3743_213+3744delinsAG	XP_011543325.1:n.213+3743_213+3744delinsAG
XM_011545023.2:c.213+3743_213+3744delinsAG	XP_011543325.1:n.213+3743_213+3744delinsAG
XM_017017723.1:c.351+4433_351+4434delinsAG	XP_016873212.1:n.351+4433_351+4434delinsAG
XM_017017724.1:c.351+4433_351+4434delinsAG	XP_016873213.1:n.351+4433_351+4434delinsAG
XR_001747866.1:n.366+4433_366+4434delinsAG
XR_001747867.1:n.366+4433_366+4434delinsAG
XR_001747868.1:n.377+3743_377+3744delinsAG
XR_001747869.1:n.377+3743_377+3744delinsAG
NM_021727.5:c.213+3743_213+3744delinsAG MANE Select	NP_068373.1:n.213+3743_213+3744delinsAG